Loss of Stathmin-2, a hallmark of TDP-43-associated ALS, causes motor neuropathy

Authors

Kelsey L Krus, Washington University School of Medicine in St. Louis
Amy Strickland, Washington University School of Medicine in St. Louis
Yurie Yamada, Washington University School of Medicine in St. Louis
Laura Devault, Washington University School of Medicine in St. Louis
Robert E Schmidt, Washington University School of Medicine in St. Louis
A Joseph Bloom, Washington University School of Medicine in St. Louis
Jeffrey Milbrandt, Washington University School of Medicine in St. Louis
Aaron DiAntonio, Washington University School of Medicine in St. Louis

Journal

Cell Reports

Publication Date

6-28-2022

Volume

39

Issue

13

First Page

111001

Document Type

Open Access Publication

DOI

10.1016/j.celrep.2022.111001

Rights and Permissions

Krus KL, Strickland A, Yamada Y, Devault L, Schmidt RE, Bloom AJ, Milbrandt J, DiAntonio A. Loss of Stathmin-2, a hallmark of TDP-43-associated ALS, causes motor neuropathy. Cell Rep. 2022 Jun 28;39(13):111001. doi: 10.1016/j.celrep.2022.111001. Copyright 2022 The Author(s). This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/)

Recommended Citation

Krus, Kelsey L; Strickland, Amy; Yamada, Yurie; Devault, Laura; Schmidt, Robert E; Bloom, A Joseph; Milbrandt, Jeffrey; and DiAntonio, Aaron, "Loss of Stathmin-2, a hallmark of TDP-43-associated ALS, causes motor neuropathy." Cell Reports. 39, 13. 111001 (2022).
https://digitalcommons.wustl.edu/oa_4/1335

Department

ICTS (Institute of Clinical and Translational Sciences)

Additional Links

Supplemental material is available for this article at publisher site.